Share Email Print

Proceedings Paper

Performance and applications of the dynamic focus scanning laser imaging system
Author(s): Bradley D. Clymer; Jogikal M. Jagadeesh; Gregory S. Bergmann; L. David Tomei
Format Member Price Non-Member Price
PDF $17.00 $21.00

Paper Abstract

A multipurpose digital imaging device has been developed for applications in quantitative densitometry, light scatter detection and fluorescence emission measurement. The Scanning Laser Imaging (SLI) device consists of a three-dimensional laser beam controller, a fiber optic faceplate coupler, a specially designed photodetector assembly and a support computer that has interactive control over the beam positioner. Image information is collected as measurement of either total forward light loss, forward direction scattering or fluorescent emission, depending on the nature of the biological target and the configuration of the detection assembly. Signal output from the bulk photodetector is digitized and assigned to the corresponding pixel location illuminated by the laser spot. The target and detector assembly are stationary while the laser spot is scanned in a programmed pattern. Areas up to 16 cm2 are scanned at a rate of 5.1 x iO pixels/s with 12 bits gray level detection range per pixel. Typically, 1024 x 1024 pixels are captured in less than 30 seconds and stored for display, processing or archiving. Spatial resolution for image reconstruction is a function of laser spot size and has been demonstrated to 3 pm. Rescan and arbitrary laser spot positioning is accomplished to within Biological, biophysical, clinical instrumentation and optical and computer engineering applications of this technology are broad. SLI methods have been developed for quantitative densitometric analysis of electrophoretic gels, thin-layer chromatography plates and autoradiographic materials generally used in molecular biology research. These applications are not well suited for conventional scanning densitometry, particularly when translucent materials such as nylon or nitrocellulose transfer membranes are used because of loss in resolution due to scattering. The SLI spatial resolution is not affected significantly by such scatter. Other quantitative analysis such as measurement of immunofluorescent and immunochemical staining of cells from blood samples and tissue sections can be performed with the SLI device. These applications are poorly suited for traditional flow cytometry, which requires dispersal of individual cells from the tissue. In addition to imaging, the SLI device is capable of detecting and analyzing the occurrence of very rare events. It is routinely capable of scanning a large transparent or translucent target, detecting submicron particles and recording the position of the particles to within approximately 1 pm. The system will detect and locate a single submicron particle placed anywhere on a 800 mm2 surface, a task analogous to locating a standard typewritten character placed on a football field, within 30 seconds.

Paper Details

Date Published: 1 July 1990
PDF: 12 pages
Proc. SPIE 1201, Optical Fibers in Medicine V, (1 July 1990); doi: 10.1117/12.17593
Show Author Affiliations
Bradley D. Clymer, Ohio State Univ. (United States)
Jogikal M. Jagadeesh, Ohio State Univ. (United States)
Gregory S. Bergmann, Ohio State Univ. (United States)
L. David Tomei, Ohio State Univ. (United States)

Published in SPIE Proceedings Vol. 1201:
Optical Fibers in Medicine V
Abraham Katzir, Editor(s)

© SPIE. Terms of Use
Back to Top